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Following achievements in Asia, Roche's PNH treatment drug PIASKY (crovalimab) received its first FDA approval. This approval has spiked the competition between Roche and current market leader AstraZeneca. Additionally, the other pharma companies also geared up to launch their respective lead assets. LAS VEGAS, Sept. 2, 2024 /PRNewswire/ -- Paroxysmal nocturnal hemoglobinuria (PNH), a rare disorder, shows a triad of features: intravascular hemolysis, thromboembolic events, and cytopenia. Manifestations vary among patients, making classification based on typical presentations challenging due to the disease's unpredictable nature. In 2023, the Paroxysmal Nocturnal Hemoglobinuria diagnosed prevalent cases were ~12,000 cases in the 7MM, which might reach ~13,000 cases by 2034. In the 7MM, the highest number of paroxysmal nocturnal hemoglobinuria diagnosed prevalent cases were observed in the US. Until 2007, PNH was a devastating disease without treatment for hemolysis and thrombosis, the leading cause of death in patients. However, the last decade saw a revolutionary shift with the advent of the anti-C5 agent eculizumab. It significantly reduced hemolysis, decreased transfusion dependency, and, crucially, lowered the thrombosis rate. The disease-modifying therapeutic strategy for paroxysmal nocturnal hemoglobinuria includes complement inhibition therapy, with drugs like SOLIRIS, ULTOMIRIS, and EMPAVELI approved by the FDA, and considered the gold standard. SOLIRIS, the pioneering therapy for PNH, was succeeded by ULTOMIRIS, both developed by Alexion Pharmaceuticals, offering C5 inhibitors as essential therapeutic options. Recent approvals of factor B and D inhibitors like FABHALTA (iptacopan) in the US and VOYDEYA (danicopan) in Japan aim to offer improved treatment with fewer side effects. Learn more about the FDA-approved paroxysmal nocturnal hemoglobinuria drugs @ Drugs for Paroxysmal Nocturnal Hemoglobinuria Treatment The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) recommended crovalimab for treating PNH in adults and adolescents aged 12 and above in June 2024, based on findings from the global Phase III COMMODORE 2 clinical trial. The FDA accepted a biologics license application for crovalimab in September 2023 and subsequently approved it in June 2024 for treating PNH in adults and adolescents aged 13 years and older. Genentech, a subsidiary of Roche, has made the drug available in the US. In Japan, Chugai Pharmaceutical submitted a new drug application for PiaSky to the Japan Ministry of Health, Labour, and Welfare (MHLW) in June 2023. The drug was approved in March 2024 and launched in May 2024 for patients with PNH aged 12 years and above. In February 2024, China's National Medical Products Administration (NMPA) approved crovalimab for treating PNH in adults and adolescents aged 12 years and older who have not previously received complement inhibitor treatment, following a priority review that began in August 2022. PiaSky is also undergoing review by other regulatory authorities, including those in Europe and Taiwan. To know more about paroxysmal nocturnal hemoglobinuria treatment options, visit @ New Treatment for Paroxysmal Nocturnal Hemoglobinuria The paroxysmal nocturnal hemoglobinuria market is crowded with so many companies working in the domain. Emerging PNH therapies include Pozelimab (REGN3918) + Cemdisiran, OMS906, NM8074 (ruxoprubart), and others, reflecting a dynamic evolution in treatment strategies. Discover which therapies are expected to grab major paroxysmal nocturnal hemoglobinuria market share @ Paroxysmal Nocturnal Hemoglobinuria Market Report Pozelimab is a novel, fully human monoclonal antibody currently under investigation. It aims to inhibit complement factor C5, thereby preventing the destruction of red blood cells (hemolysis) responsible for symptoms in conditions like Paroxysmal Nocturnal Haemoglobinuria (PNH) and other diseases influenced by complement pathway activity. This IgG4 antibody binds tightly to both wild-type and variant forms of human C5, effectively blocking its function. In its ongoing development, pozelimab is also being studied in combination with Alnylam's cemdisiran, a siRNA C5 inhibitor. This investigational combination therapy is aimed at treating various complement-mediated disorders, including PNH and myasthenia gravis. OMS-906 is currently being developed to treat paroxysmal nocturnal hemoglobinuria (PNH), complement 3 glomerulopathy (C3G), idiopathic immune complex-mediated glomerulonephritis (ICGN), and arthritis. It can be administered either subcutaneously or intravenously. This drug candidate is a monoclonal antibody designed to target mannan-binding lectin serine protease 3 (MASP-3) to exert its therapeutic effects. Discover more about drugs for paroxysmal nocturnal hemoglobinuria in development @ Paroxysmal Nocturnal Hemoglobinuria Clinical Trials The anticipated launch of these emerging therapies for paroxysmal nocturnal hemoglobinuria are poised to transform the market landscape in the coming years. As these cutting-edge therapies continue to mature and gain regulatory approval, they are expected to reshape the paroxysmal nocturnal hemoglobinuria market landscape, offering new standards of care and unlocking opportunities for medical innovation and economic growth. DelveInsight estimates that in 2023, the total paroxysmal nocturnal hemoglobinuria market size in the 7MM was USD ~1.4 billion, which is expected to reach USD ~2.5 billion by 2034. This growth can be attributed to the advances in disease mechanisms that drive new diagnostics and therapeutics, fueling drug development. Additionally, the PNH market foresees positive growth, propelled by increasing cases and upcoming therapies in the forecast period. DelveInsight's latest published market report titled as Paroxysmal Nocturnal Hemoglobinuria Market Insight, Epidemiology, and Market Forecast – 2034 will help you to discover which market leader is going to capture the largest market share. The report provides comprehensive insights into the paroxysmal nocturnal hemoglobinuria country-specific treatment guidelines, patient pool analysis, and epidemiology forecast to help understand the key opportunities and assess the market's underlying potential. The paroxysmal nocturnal hemoglobinuria market report proffers epidemiological analysis for the study period 2020–2034 in the 7MM segmented into: Total Diagnosed Prevalent Cases of PNH Gender-specific Cases of PNH The report provides an edge while developing business strategies by understanding trends shaping and driving the 7MM paroxysmal nocturnal hemoglobinuria market. Highlights include: 11-year Forecast 7MM Analysis Epidemiology-based Market Forecasting Historical and Forecasted Market Analysis upto 2034 Emerging Drug Market Uptake Peak Sales Analysis Key Cross Competition Analysis Industry Expert's Opinion Access and Reimbursement Download this paroxysmal nocturnal hemoglobinuria market report to assess the epidemiology forecasts, understand the patient journeys, know KOLs' opinions about the upcoming treatment paradigms, and determine the factors contributing to the shift in the paroxysmal nocturnal hemoglobinuria market. Also, stay abreast of the mitigating factors to improve your market position in the paroxysmal nocturnal hemoglobinuria therapeutic space. Related Reports Paroxysmal Nocturnal Hemoglobinuria Epidemiology Forecast Paroxysmal Nocturnal Hemoglobinuria Epidemiology Forecast – 2032 report delivers an in-depth understanding of the disease, historical and forecasted paroxysmal nocturnal hemoglobinuria epidemiology in the 7MM, i.e., the United States, EU5 (Germany, Spain, Italy, France, and the United Kingdom), and Japan. Paroxysmal Nocturnal Hemoglobinuria Pipeline Paroxysmal Nocturnal Hemoglobinuria Pipeline Insight – 2024 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key paroxysmal nocturnal hemoglobinuria companies, including Biocad, AKARI Therapeutics, Amgen, MorphoSys, Ra Pharmaceuticals, Alnylam Pharmaceuticals, Arrowhead Pharmaceuticals, among others. Aplastic Anemia Market Aplastic Anemia Market Insights, Epidemiology, and Market Forecast – 2034 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key aplastic anemia companies, including Pfizer, BioLineRx Ltd., Regeneron Pharmaceuticals, Gamida Cell, Elixirgen, Hangzhou Zede Pharmaceutical Technology, Cellenkos, Hemogenyx Pharmaceuticals, among others. Aplastic Anemia Pipeline Aplastic Anemia Pipeline Insight – 2024 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key aplastic anemia companies, including Pfizer, BioLineRx, Ltd., Regeneron Pharmaceuticals, Gamida Cell, Elixirgen, among others. About DelveInsight DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports pharma companies by providing comprehensive end-to-end solutions to improve their performance. Get hassle-free access to all the healthcare and pharma market research reports through our subscription-based platform PharmDelve . Contact Us Shruti Thakur [email protected] +14699457679 Logo: SOURCE DelveInsight Business Research, LLP

The treatment landscape for KRAS-mutant cancers has been rapidly evolving, with several promising advancements in recent years. The KRAS inhibitors market is expected to grow significantly in the coming years, driven by the increasing incidence of cancer and the growing demand for personalized cancer treatments, ongoing research and clinical trials have identified potential treatment strategies. LAS VEGAS, July 10, 2023 /PRNewswire/ -- DelveInsight's KRAS Inhibitors Market Insights report includes a comprehensive understanding of current treatment practices, emerging KRAS inhibitors, market share of individual therapies, and current and forecasted market size from 2019 to 2032, segmented into 7MM [the United States, the EU4 (Germany, France, Italy, and Spain), the United Kingdom, and Japan]. Key Takeaways from the KRAS Inhibitors Market Report As per DelveInsight analysis, the KRAS inhibitors market size in the 7MM was approximately USD ~240 million in 2022. According to the assessment done by DelveInsight, the total KRAS-mutated cases in the 7MM comprised more than ~ 490,000 cases in 2022 and are projected to increase during the forecast period. Leading inhibitors companies such as Novartis, Roche, Genentech, Verastem Oncology, Revolution Medicines, Cardiff Oncology, Immuneering Corporation, Jacobio Pharmaceuticals, BridgeBio Pharma, Mirati Therapeutics, Deciphera Pharmaceuticals, Elicio Therapeutics, InventisBio, Gritstone Bio, D3 Bio, and others are developing novel KRAS inhibitors that can be available in the KRAS inhibitors market in the coming years. The promising KRAS inhibitors in the pipeline include JDQ443, Divarasib, Avutometinib (VS-6766), RMC-4630, Onvansertib, IMM-1-104, Glecirasib (JAB-21822), BBP-398, MRTX1133, DCC-3116, ELI-002, D-1553, SLATE-KRAS, D3S-001, and others. Discover which therapies are expected to grab the major KRAS inhibitors market share @ KRAS Inhibitors Market Report KRAS Inhibitors Overview KRAS is a member of the RAS superfamily of small GTP-binding proteins known as RAS-like GTPases. The oncogene rat sarcoma virus (RAS) acts as a signal transducer, influencing cell proliferation, differentiation, and survival in both normal and malignant cells. The most often mutated RAS gene is KRAS, followed by NRAS and HRAS. The human KRAS gene is found on chromosome 12p12.1. It is encoded by six exons, which are positioned at locations 12 and 13 in exon 1 and, less commonly, at codons 61, 63, 117, 119, and 146. KRAS mutations can be identified through genetic sequencing of tumor tissue or through the use of a liquid biopsy. KRAS testing requests for patients are often initiated by the doctor. Typically, the examination is done on tumor tissue extracted from the patient through a previous surgery or biopsy operation. Adjuvant therapy is usually required for patients having KRAS testing who have advanced tumors. KRAS Inhibitors Epidemiology Segmentation DelveInsight estimates that there were approximately ~ 490,000 total KRAS-mutated cases in the 7MM in 2022. KRAS mutations are seen most frequently in pancreatic cancer, followed by CRC and NSCLC. The most frequent KRAS variant observed in NSCLC is G12C. In addition, the most common KRAS variation in CRC and pancreatic cancer is G12D. In the United States, KRASG12C is present in ~37% of NSCLC cases. The highest rates of KRASG12D, i.e., ~42% and 30%, were found in pancreatic cancer and CRC, respectively. The KRAS inhibitors market report proffers epidemiological analysis for the study period 2019–2032 in the 7MM segmented into: Total Incident Cases of NSCLC, CRC, and Pancreatic Cancer Total KRAS Incident Cases in NSCLC, CRC, and Pancreatic Cancer Total KRAS Variant Cases in NSCLC, CRC, and Pancreatic Cancer KRAS Inhibitors Treatment Market Treatment choices for KRAS-mutant cancer are determined on the type of cancer, stage of the disease, and individual patient factors. The treatment landscape for KRAS-mutated cancer has been evolving. Chemotherapy drugs such as platinum-based agents (cisplatin, carboplatin), taxanes (paclitaxel, docetaxel), and others may be used to treat KRAS-mutant tumors. Chemotherapy is frequently used in conjunction with other treatments, such as targeted therapies or immunotherapies. Certain targeted therapy may be used depending on the type of cancer and the concomitant genetic changes. In colon cancer with KRAS mutations, for example, anti-EGFR antibodies (cetuximab, panitumumab) may be administered if the KRAS mutation is wild-type at codons 12 and 13. In some circumstances, alternative targeted treatments that inhibit downstream signaling pathways (such as MEK inhibitors) or angiogenesis pathways (such as anti-VEGF therapies) may be considered. Immune checkpoint inhibitors, such as pembrolizumab and nivolumab, and CTLA-4 inhibitors (ipilimumab), have transformed cancer treatment. While immunotherapy may not directly target KRAS mutations, it can improve the immune system's ability to identify and fight cancer cells. For KRAS-mutant tumors, clinical trials are looking into combining immunotherapy with other targeted medicines like chemotherapy. The FDA granted accelerated clearance to LUMAKRAS (sotorasib, Amgen) in May 2021 for the treatment of people with advanced non-small cell lung cancer (NSCLC) who have a KRAS G12C mutation and have had at least one prior systemic therapy. The FDA granted accelerated approval for KRAZATI (adagrasib) in December 2022, a targeted treatment option for adult patients with KRASG12C-mutated locally advanced or metastatic non-small cell lung cancer (NSCLC), as determined by an FDA-approved test, who have received at least one prior systemic therapy. Mirati filed a Marketing Authorization Application (MAA) in the EU in May 2022. To know more about KRAS inhibitors, visit @ KRAS Inhibitors Treatment Key KRAS Inhibitors Therapies and Companies JDQ443: Novartis Divarasib: Roche/Genentech Avutometinib (VS-6766): Verastem Oncology RMC-4630: Revolution Medicines Onvansertib: Cardiff Oncology IMM-1-104: Immuneering Corporation Glecirasib (JAB-21822): Jacobio Pharmaceuticals BBP-398: BridgeBio Pharma (Navire Pharma) MRTX1133: Mirati Therapeutics DCC-3116: Deciphera Pharmaceuticals ELI-002: Elicio Therapeutics D-1553: InventisBio SLATE-KRAS: Gritstone Bio D3S-001: D3 Bio Learn more about the FDA-approved KRAS inhibitors @ KRAS Inhibitors Drugs KRAS Inhibitors Market Dynamics The dynamics of the KRAS inhibitors market are anticipated to change in the coming years. Historically, KRAS mutations were thought to be difficult to target, and effective treatments for KRAS-mutant tumors were scarce. As a result, there is a substantial unmet need for effective therapies, resulting in high KRAS inhibitors market demand. In addition, research advances have led to the identification of possible treatment targets and techniques for KRAS-mutant malignancies. The continued development of targeted therapies, such as KRAS-G12C and Pan-KRAS inhibitors, provides a considerable KRAS inhibitors market opportunity. However, despite decades of research, there have been few viable tactics for targeting KRAS mutations, with the exception of recent breakthroughs like sotorasib and adagrasib, which have been approved to target a specific mutant version of KRAS known as KRAS (G12C). Because of its inherent properties, specifically targeting KRAS has proven to be a hard challenge. As a result, scientists have looked into alternative tactics such as targeting downstream signaling molecules, using epigenetic methods such as telomerase inhibitors and RNA interference, and adopting synthetic lethality procedures involving cyclin-dependent kinase inhibitors. Furthermore, as our understanding of KRAS biology grows, more companies and institutions are entering the sector to explore therapeutics for KRAS-mutant malignancies. The KRAS inhibitors market may grow highly competitive, with numerous companies contending for KRAS inhibitors market share. Moreover, Amgen and Mirati Therapeutics are at the forefront of the race to discover KRAS inhibitors for cancer treatment. However, their present prospects are mainly focused on G12C-mutant tumors, leaving a major gap in tackling other KRAS variations. This represents a significant unmet need in the profession, given no approved treatments are currently available for other variations. Recognizing this difficulty, multiple prominent players are currently investigating alternate KRAS variations and expanding their research to cover tumors other than NSCLC. This shift in focus has the potential to lead to the development of successful medicines that can address a broader spectrum of KRAS mutations and target numerous cancer types. Scope of the KRAS Inhibitors Market Report Therapeutic Assessment: KRAS Inhibitors current marketed and emerging therapies KRAS Inhibitors Market Dynamics: Attribute Analysis of Emerging KRAS Inhibitors Drugs Competitive Intelligence Analysis: SWOT analysis and Market entry strategies Unmet Needs, KOL's Views, Analyst's Views, KRAS Inhibitors Market Access and Reimbursement Discover more about KRAS inhibitors drugs in development @ KRAS Inhibitors Clinical Trials Table of Contents Related Reports JAK Inhibitors Competitive Landscape JAK Inhibitors Competitive Landscape – 2023 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key JAK inhibitors companies, including Pfizer, Sierra Oncology, Theravance Biopharma, Dizal Pharmaceutical, Aclaris Therapeutics, Celon Pharma, Incyte Corporation, AbbVie, Galapagos, among others. TIGIT Inhibitors Competitive Landscape TIGIT Inhibitors Competitive Landscape – 2023 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key TIGIT inhibitors companies, including Merck Sharp & Dohme, Bristol-Myers Squibb, BeiGene, Arcus Biosciences, iTeos Therapeutics, Mereo BioPharma, Phio Pharmaceuticals, Bio-Thera Solutions, Compugen, among others. Checkpoint Inhibitors Competitive Landscape Checkpoint Inhibitors Competitive Landscape – 2023 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key checkpoint inhibitors companies, including BeBetter Med, BIOCAD, CanBas Co., Ltd., Laekna Therapeutics, Genentech, Alphamab Oncology, Hangzhou Sumgen Biotech, Harbour BioMed, Aurigene Discovery Technologies, BeiGene, Apollomics, BCN Biosciences, Phio Pharmaceuticals, Atridia, Jiangsu HengRui Medicine, EMD Serono, Innovent Biologics, Agenus, among others. PD-1 and PD-L1 Inhibitors Competitive Landscape PD-1 and PD-L1 Inhibitors Competitive Landscape – 2023 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key PD-1 and PD-L1 inhibitors companies, including Merck, Laekna Therapeutics, Genentech, Tracon Pharmaceuticals Inc., Celgene, MedImmune, Hangzhou Sumgen Biotech, among others. About DelveInsight DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports pharma companies by providing comprehensive end-to-end solutions to improve their performance. Get hassle-free access to all the healthcare and pharma market research reports through our subscription-based platform PharmDelve . Contact Us Shruti Thakur [email protected] +1(919)321-6187 Logo: SOURCE DelveInsight Business Research, LLP

Platelet-rich plasma (PRP) demand is being driven primarily by an increase in the number of patients suffering from orthopedic diseases, sports injuries, acute and chronic wounds, gynecological diseases, and urological diseases, among other conditions. Furthermore, the increasing demand for platelet-rich plasma in various aesthetic procedures as well as increasing product launches and approval by leading companies such as Johnson & Johnson, Zimmer Biomet, Arthrex, Terumo Corporation, Stryker, and others, are all contributing to the overall growth of the platelet-rich plasma market. LAS VEGAS, June 27, 2023 /PRNewswire/ -- DelveInsight's Platelet-Rich Plasma Market Insights report provides the current and forecast market analysis, individual leading platelet-rich plasma companies' market shares, challenges, platelet-rich plasma market drivers, barriers, trends, and key market Platelet-Rich Plasma companies in the market. Key Takeaways from the Platelet-Rich Plasma Market Report As per DelveInsight estimates, North America is anticipated to dominate the global platelet-rich plasma market during the forecast period. Notable platelet-rich plasma companies such as Johnson & Johnson, Zimmer Biomet, Arthrex, Terumo Corporation, Stryker, Dr. PRP USA LLC., Juventix Regenerative Medical, LLC., EmCyte Corporation, Apex Biologix, Celling Biosciences, Isto Biologics, Exactech, Inc., Nuo Therapeutics, Inc., Regen Lab SA, CollPlant Biotechnologies Ltd., Estar Technologies Ltd., ELTEK S.P.A., Royal Biologics, PRP Concepts, Crown, and several others, are currently operating in the platelet-rich plasma market. In May 2023, Regen Lab, a global commercial-stage medical technology company specializing in the research, development, registration, manufacturing, and commercialization of proprietary tissue engineering products, announced that its best-in-class medical devices REGENKIT®, CELLULAR MATRIX fig®, and Arthrovisc® have received CE certification under the EU Medical Device Regulation 2017/745. In February 2023, Royal Biologics, a company specializing in Advanced Cellular Technologies & Enhanced Autologous Solutions, announced the commercial launch of BIOINCYTE™ PRFM, a next-generation PRP system, which converts traditional PRP to Platelet Rich Fibrin Matrix (PRFM) formulations. In October 2022, i-Stem PRP Kit Platelet Rich Plasma Therapy was launched in the UK, which is a unique, modernized anti-shake patented i-Stem PRP System, for the safe and effective treatment within the exciting field of regenerative medicine, making the treatment effective and simple. In September 2021, Royal Biologics, an ortho-biologics company focused on Autologous and Live Cellular solutions, announced FDA 510K approval of their Maxx- PRP concentration system. The system is a patented next-generation concentration device that can be used to concentrate autologous whole blood for the safe and rapid preparation of platelet-rich plasma to use point of care for mixing with autograft and/or allograft to improve handling characteristics. In February 2020, EmCyte, the world leader in platelet-rich plasma and progenitor stem cell biologics, announced FDA 510(k) clearance for its PurePRP® Supraphysiologic Concentrating System for platelet-rich plasma. The system is cleared to be used for the safe and rapid preparation of autologous platelet-rich plasma (PRP) extracted from sample of blood at the patient's point of care. To read more about the latest highlights related to the platelet-rich plasma market, get a snapshot of the key highlights entailed in the Global Platelet-Rich Plasma Market Report Platelet-Rich Plasma Overview Platelet-rich plasma (PRP) is obtained from blood. It is produced when human blood is spun down and platelet-rich plasma with platelet concentrations above normal levels is isolated. Platelets aid in blood clotting as well as the repair of tendons, muscles, and ligaments. A normal platelet count is 150,000 to 450,000 platelets per microliter of blood. Platelet-rich plasma. Platelet-rich plasma is used in a variety of operations, including shoulder rotator cuff augmentation and tendon repair. Platelets are exceptionally high in healing agents and connective tissue growth. Platelet-Rich Plasma Market Insights North America accounted for the highest proportion of the platelet-rich plasma market in 2022, accounting for 43% of all regions. PRP demand is expected to rise during the forecast period due to factors such as an aging population, an increase in traumatic injuries caused by falls, accidents, and other causes, an increase in the number of orthopedic and cosmetic procedures, and recent product launches in the region. Furthermore, increased physician and patient awareness of newly established treatment processes and technologies are likely to contribute to the growth of the North America platelet-rich plasma market. Moreover, a high disposable income, advanced healthcare infrastructure, regulatory approval for new products, and a high level of knowledge regarding ophthalmic diseases all contributed to the success of the North American platelet-rich plasma market growth. To know more about why North America is leading the market growth in the platelet-rich plasma market, get a snapshot of the Platelet-Rich Plasma Market Outlook Platelet-Rich Plasma Market Dynamics The platelet-rich plasma market is seeing increased product demand due to a variety of factors, one of which is the increased prevalence of various therapeutic indications. PRP can successfully manage pain in orthopedic conditions and treat osteoporosis. As a result of the rising prevalence of orthopedic diseases such as arthritis, tennis elbow, golfer's elbow, plantar fasciitis, rotator cuff injuries, and others, the demand for PRP therapy will rise, as will the demand for PRP systems and kits used in PRP therapy. Moreover, PRP therapy for fat grafts improves fat graft survival, reduces bruising and inflammation, and makes fat graft application easier. Furthermore, platelets-rich plasma is reported to accelerate healing by minimizing postoperative edoema and bleeding, making it useful in a variety of cosmetic operations. Thus, the increasing demand for platelet-rich plasma in various aesthetic operations such as cosmetic facials, facial rejuvenation, acne scars, facial scarring, facelift, and others will have a favorable impact on the platelet-rich plasma market in the approaching years. Furthermore, PRP is extensively utilized for hair restoration in addition to facial surgeries. PRP can be used as a monotherapy or as an addition to conventional therapy or hair transplantation to treat hair loss, including androgenetic alopecia and female pattern hair loss. However, the presence of alternative treatment choices, many sessions, resulting in high therapy costs, and other factors may limit the growth of the platelet-rich plasma market. Additionally, during the COVID-19 pandemic, the platelet-rich plasma market was greatly impacted. The pandemic's spread resulted in the cancellation of outpatient consultations as well as the suspension of non-emergency hospitalization and treatment procedures for a variety of conditions such as orthopedic and sports injuries, gynecological, urological, cosmetic, and others. As a result, the number of individuals receiving standard therapy for the aforementioned illnesses has decreased. Furthermore, several elective procedures were postponed while the care of patients infected with coronavirus was prioritized. Furthermore, supply chain, raw material, and other resource constraints interrupted device manufacturing, resulting in a shortage of devices and kits on the market. However, the invention of the COVID-19 vaccine triggered the economic recovery process. Furthermore, with the easing of lockdown restrictions and the return of normalcy in the economic landscape, the process of resumption of regular healthcare services such as outpatient visits for various treatments, therapies, and surgeries for the aforementioned ailments began, bringing the platelet-rich plasma market back on track. Get a sneak peek at the platelet-rich plasma market dynamics @ Platelet-Rich Plasma Market Dynamics Analysis Platelet-Rich Plasma Market Assessment Platelet-Rich Plasma Market Segmentation Platelet-Rich Plasma Market Segmentation By Product Type: PRP Systems and PRP Kits Platelet-Rich Plasma Market Segmentation By PRP Type: Pure Platelet Rich Plasma, Leukocyte Rich Plasma, and Others Platelet-Rich Plasma Market Segmentation By Application: Orthopedic, Sports Medicine, Cosmetic Surgery, and Others Platelet-Rich Plasma Market Segmentation By End User: Hospitals, Clinics, and Others Platelet-Rich Plasma Market Segmentation By Geography: North America, Europe, Asia-Pacific, and Rest of World Porter's Five Forces Analysis, Product Profiles, Case Studies, KOL's Views, Analyst's View Which MedTech key players in the platelet-rich plasma market are set to emerge as the trendsetter explore @ Platelet-Rich Plasma Companies Table of Contents Related Reports Psoriatic Arthritis Pipeline Psoriatic Arthritis Pipeline Insight – 2023 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key psoriatic arthritis companies, including Mylan, Celltrion, Pfizer, Amgen, among others. Psoriatic Arthritis Market Psoriatic Arthritis Market Insights, Epidemiology, and Market Forecast – 2032 report deliver an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key psoriatic arthritis companies, including Mylan, Celltrion, Pfizer, Amgen, among others. Psoriasis Pipeline Psoriasis Pipeline Insight – 2023 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key psoriasis companies, including Mylan, Biocad, Bristol-Myers Squibb, Celltrion, Coherus BioSciences, among others. Psoriasis Market Psoriasis Market Insights, Epidemiology, and Market Forecast – 2032 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key psoriasis companies, including Mylan, Biocad, Bristol-Myers Squibb, Celltrion, Coherus BioSciences, among others. About DelveInsight DelveInsight is a leading Business Consultant, and Market Research firm focused exclusively on life sciences. It supports pharma companies by providing comprehensive end-to-end solutions to improve their performance. Contact Us Shruti Thakur [email protected] +1(919)321-6187 Logo: SOURCE DelveInsight Business Research, LLP